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2nd Shift QA Manufacturing SpecialistHarrow Defunct • United States
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2nd Shift QA Manufacturing Specialist

Harrow Defunct
  • US
    United States
  • US
    United States
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À propos

2nd Shift QA Manufacturing Specialist
Harrow is a leading provider of ophthalmic disease management solutions in North America. Harrow is an incredible entrepreneurial company – where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow's values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to innovation, patient access to affordable medicines, and our track record of having never turned down an ophthalmologist doing mission work around the world – providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need. Harrow's ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including: An expanding Retina Portfolio including IHEEZO®, TRIESENCE®, BYOOVIZ™, and OPUVIZ™ A broad Dry Eye Disease product line, led by VEVYE® and bolstered by well-known adjacent ocular surface disease products such as FLAREX® and FRESHKOTE® A peri-operative Surgical product line, led by TRIESENCE® and BYQLOVI™ A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO®, NATACYN®, and VERKAZIA® A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01 The hours for this position are from 3pm - 1:30am. Job Summary This position will ensure that the operations follow the cGMP standards promulgated under Section 503B of the US Food, Drug & Cosmetic Act. The QA Manufacturing Specialist will provide Quality oversight of the Manufacturing and Production areas, including compounding, filling, inspecting, and labeling/packaging. Management includes the periodic review of in-process activities such as cleaning, weighing, aseptic filling, material status verification, compounding, batch record documentation accuracy, logbook documentation accuracy, and room/line clearances. Core Responsibilities Provides Quality oversight of Production activities, including compounding, aseptic filling, inspection, and labeling/packaging on the floor. Provides Quality oversight of cleaning activities to ensure compliance with cleaning requirements. Product label review and approval. Oversight and confirmation compliance with Filling Operations, including line clearance, material status, aseptic technique, in-process quality attribute testing, documentation on forms, and batch records. Verification of proper gowning by all personnel in all areas of Production. Generation of deviations, issuance of CAPAs, and Change Controls in response to observations. Oversee all Quality aspects on the floor. Participate in regulatory audits if required. Performs or assists process owners with the root cause analysis. Responsible for generating deviations and change controls when required. Performs duties following established company procedures and policies; performs other duties as assigned. Qualifications & Requirements 3-5 years of progressive experience in cGMP quality operations and FDA regulations, a 503B outsourcing facility, aseptic/parenteral manufacturing/development environment, or equivalent technical experience. High school degree BS in the Scientific field preferred Three-plus years of experience with aseptic drug product manufacturing is required. A fundamental, working knowledge of safety, quality systems, and quality assurance concepts are required, including the application of current Good Manufacturing Practices and Good Documentation Practices. Strong familiarity with manufacturing processes, operations, automation, and equipment/facilities. Ability to complete tasks with little direction or need for supervisory follow-up. Strong written, verbal, and presentation communication skills. Strong computer skills in database management and documentation preparation (Word, PowerPoint, Excel, and others must be able to learn additional software as required). Ability to think creatively in confronting new issues and pursuing novel approaches to old problems. Ability to work under pressure, meet deadlines and exercise sound business judgment with critical thinking skills and high ethical standards. Work schedule flexibility. Position Type On-Site Full-time position in a manufacturing facility with regular operations between M-F in our Ledgewood, NJ location. Working hours may vary from several hours before opening to several hours after closing. Additionally, weekend hours may be needed depending upon workload demands. Along with possible rotating shifts and holiday work during inclement weather. Travel Up to 5%
  • United States

Compétences linguistiques

  • English
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